Potential of Nb2O5 nanofibers in photocatalytic degradation of organic pollutants.

Various photocatalytic nanomaterials for environmental remediation have been promoted due to the pollution caused by different organic pollutants. In this study, Nb2O5 nanofibers were obtained by electrospinning technique, presenting controlled crystallinity and high specific surface area to improve the photoactivity response. The structural characterization indicated Nb2O5 nanofibers with orthorhombic phase formation. The photoluminescence measurements showed different energy levels contributing to the electronic transition events. The nanofibers with a bandgap up to 3.6 eV were applied to photocatalysis of dyes (rhodamine B (RhB) or methylene blue (MB)) and fluoxetine (FLX), listed as an emergent pollutant. In the optimized condition (pH = 9), the RhB and MB photocatalysis was 59% and 93% more efficient than photolysis due to ζ = - 50 mV ± 5 for EtOH_550 sample increased interaction with MB (cationic) compared to RhB unprotonated (pKa = 3.7). Therefore, FLX (pKa = 10.7) was selected due to protonated form at pH = 9 and showed 68% ± 1 adsorption in 30 min for EtOH_550. The FLX photocatalytic degradation under UV light irradiation was up to 17% higher than the photolytic degradation. The formation of hydroxyl radicals in the photocatalytic system (EtOH_550) was proven by the Coumarine probe assay, corroborating with the greater amount of α-[2-(methylamino)ethyl]benzylalcohol (MAEB), a by-product obtained after FLX oxidation. Additionally, the material achieved specific catalytic activity for the different organic compounds (RhB, MB, or FLX). Therefore, Nb2O5 nanofibers were efficient for degrading three different pollutants under UV light, proving a viable alternative for environmental remediation.

N-compounds speciation analysis in environmental samples using ultrasound-assisted solid-liquid extraction and non-chromatographic techniques.

A fast, efficient, and non-chromatographic method was presented in this study for nitrite, nitrate, and p-nitrophenol (N-compounds) extraction and speciation analysis of environmental samples. By applying ultrasound-assisted solid-liquid extraction (USLE), analytes were efficiently extracted from water, soil, or sediment collected in areas of environmental disaster. These analytes were selectively converted to NO(g) through UV photolysis (NO3-), H2O2/UV photocatalysis (PNP), and direct conversion (NO2-). Following conversion, NO(g) was separated from the liquid phase and determined by high-resolution continuum source molecular absorption spectrometry (HR-CS MAS). The LODs obtained were 0.097 ± 0.004 mg L-1 for nitrite, 0.119 ± 0.004 mg L-1 for nitrate, and 0.090 ± 0.006 mg L-1 for p-nitrophenol. On applying this speciation method to environmental samples, concentrations were found to be up to 0.99 ± 0.03 mg L-1 (NO2-), 49.80 ± 2.5 mg L-1 (NO3-), and 0.10 ± 0.02 mg L-1 (PNP). Finally, addition/recovery study of real water, soil, and sediment samples showed 101 ± 2% recovery for NO2-, 100 ± 1% for NO3-, and 96 ± 5% for PNP.

Nb2O5 nanoparticles decorated with magnetic ferrites for wastewater photocatalytic remediation.

Nanotechnology has been studied on environmental remediation processes to foster greater photocatalysts efficiency and reuse in wastewater. This study investigated the photocatalytic efficiency and viability of niobium pentoxide (Nb2O5) nanoparticles decorated with magnetic ferrite (cobalt ferrite (CoFe2O4) or magnesium ferrite (MgFe2O4)) for atrazine photodegradation. Thus, the decorated Nb2O5 was synthesized by the polymeric precursor method, forming nanoparticles with sizes ranging from 25 to 50 nm. Nanocomposite elementary analyses showed a homogeneous distribution of elements on all particles surface. Efficient magnetic saturation was observed for pure CoFe2O4 (53 emu g-1) and MgFe2O4 (19 emu g-1) nanoparticles, promoting the magnetic removal of Nb2O5:CoFe2O4 and Nb2O5:MgFe2O4 nanocomposites. Photocatalytic assays showed 88% efficiency for atrazine photodegradation with all nanomaterials, which represented a 21% increase compared to photolysis in the 1st cycle. The magnetic nanocomposites when applied to a 5th cycle maintained the atrazine photodegradation activity. In this way, magnetic Nb2O5-based nanocomposites decorated with ferrite nanoparticles showed an efficient photocatalytic response, in addition to posterior magnetic removal from the aqueous medium. Therefore, the evaluated magnetic Nb2O5 nanocomposites may be an alternative to enhance the wastewater removal process and foster the reuse in advanced oxidative processes.

UV photochemical hydride generation using ZnO nanoparticles for arsenic speciation in waters, sediments, and soils samples.

The environmental disasters that occurred due to the leakage of mining waste in Mariana-MG (2015) and Brumadinho-MG (2019), located in Brazil, attracted the attention of the scientific community. This designated efforts to investigate the environmental consequences of toxic waste in the affected ecosystem. Therefore, a simple, easily executed and accessible method was presented for arsenic speciation [As(III), As(V), and DMA]. Using an atomic absorption spectrometer coupled to the hydride generation system, the heterogeneous photocatalysis was applied in the reduction of As(V) and DMA to As(III). After the optimization, a calibration curve was constructed, with LODs equivalent to 3.20 µg L-1 As(III), 3.86 µg L-1 As(V), and 6.68 µg L-1 DMA. When applying the method for quantification in environmental samples, a concentration of up to 103.1 ± 9.4 µg L-1 As(V) was determined for surface water samples. The soil samples, 84.1 ± 3.6 µg L-1 As(III) and 112.4 ± 9.9 µg L-1 As(V) were quantified, proving the contamination of the ecosystems impacted by the environmental disasters. We proceeded the study through an addition/recovery method with samples of water, soil, and sediments (collected from impacted environments). Recovery values were equivalent to 99.0% for As(III), 93.8% for As(V), and 99.2% for DMA. Graphical abstract Photocatalytic reduction mechanism of As(V) and DMA to As(III) by heterogeneous photocatalysis.

Growth of the aquatic macrophyte Ricciocarpos natans (L.) Corda in different temperatures and in distinct concentrations of aluminum and manganese.

One of the consequences of global mining is the exposure of metals into the environment, caused by the rupture of tailings dams. Excess of metals, such as aluminum (Al) and manganese (Mn) can cause serious damage to fauna and flora. The presence of these metals, associated with the temperature increase that occurs nowadays can potentially increase biochemical and metabolic rates in plant tissues and may affect growth. Therefore, the objective of this work was to evaluate the toxicity of the metals Al and Mn into the biomass' growth of the macrophyte Ricciocarpos natans, under two temperatures (25 and 27 °C). R. natans individuals (n = 10 ± 0.5 cm wide) were exposed during 30 days to Al (1.5; 2.5 and 5.0 mg L-1) and Mn (0.7; 1.5 and 3.0 mg L-1) at temperatures and photoperiod-controlled germination chambers. Fresh macrophyte masses were determined gravimetrically to determine the kinetic growth using a logistic model. With that, it was noticed that the presence of Al interfered negatively in the increase of the R. natans biomass, mainly in the highest concentrations and at 27 °C. Mn, on the other hand, affected the increase in biomass, mainly in the highest concentration. As a result, the growth coefficients (µ) changed, being up to 4 times lower in the Al bioassays and up to 2 times higher than the control in the Mn bioassays. However, the dry R. natans biomass individuals that were exposed to the treatments was reduced when compared to the control, except for the lower concentration of Mn. These results contribute to the understanding of the environmental changes that can occur due to metals contained in mining tailings in aquatic ecosystems and the influence of global warming on the metabolic processes of the growth of aquatic macrophytes.

Speciation of As in environmental samples using the nano-TiO2/PCHG-FAAS online system.

This work presents an alternative method for arsenic speciation using the nano-TiO2 hydride generation photocatalytic hydride generation (PCHG) system, which is easily separated from the medium. Nano-TiO2 was studied as photocatalyst to reduction of arsenic species by UV-induced with formic acid and atomic absorption detection of different forms of arsenic [As (III), As (V), dimethylarsinic acid (DMA)] in environmental samples (water, sediment and plant). The effect of the average pH, the organic acid concentration, the ultraviolet irradiation time and their amount were investigated. With the presence of formic acid, the process was more effective in the reduction of arsenic when compared to other organic acids, mainly acetic acid. In addition, the photocatalytic hydride generation and flame atomic absorption spectrometry (nano-TiO2/PCHG-FAAS) increased the identification and quantification of different arsenic species. The ultrasound extraction procedure was used as a method to prepare samples with solutions of 1.0 mol L-1 phosphoric acid. The accuracy of the measurements (n = 12), calculated as relative standard deviation, was less than 8.6%. The detection limits for As (III) and As (total) in samples were 0.418 and 0.574 µg g-1, respectively.